The National Institutes of Health (NIH), National Cancer Institute's Early Detection Research Network (EDRN) is a cross-institutional collaborative initiative seeking to accelerate the clinical application of cancer biomarker research. Over the past decade, it has been our role, as EDRN's Informatics Center (IC), to develop a comprehensive information services infrastructure as well as a set of software tools and services to support this overall initiative. We have recently developed a novel application called the Laboratory Catalog and Archive Service (LabCAS) whose focus is to extend EDRN IC data management and processing capabilities to EDRN laboratories. By leveraging the same technologies used to manage and process NASA Earth and Planetary data sets, we offer EDRN researchers an effective way of managing their laboratory data. More specifically, LabCAS enables EDRN researchers to reliably archive their experimental data, to optionally share these data in a controlled manner with other researchers, and to gain insight into these data through highly configurable data analysis pipelines tailored to the broad range of biomarker related experiments. This particular collaboration leverages expertise from NASA's Jet Propulsion Laboratory, Vanderbilt University Medical Center, and Dartmouth Medical School, as well as builds upon existing cross-governmental collaboration between NASA and the NIH.

The dramatic increase in data in the area of cancer research has elevated the importance of effectively managing the quality and consistency of research results from multiple providers. The U.S. National Cancer Institute's Early Detection Research Network (EDRN) is a prime example of a virtual organization, sponsoring distributed, collaborative work at dozens of institutions around the country. As part of a comprehensive informatics infrastructure, The NASA Jet Propulsion Laboratory, in collaboration with Dartmouth Medical School, has developed a web application for the curation of cancer biomarker research results. In this paper, we describe and evaluate the application in the context of the EDRN content management process, and detail our experience using the tool in an operational environment to capture and annotate biomarker research data generated by the EDRN.

MOTIVATION: The radioactivity labeled DNA array platform is a robust and accurate way for a high-throughput measurement of gene expression levels in biological samples. Despite its high degree of sensitivity and reproducibility, this platform has several sources of variation. These are related to the presence of saturation effects in the array images and impede the degree of accuracy at which gene expression levels are determined. RESULTS: Here we describe a simple, but effective, approach for combining expression data from a series of autoradiographic exposures of variable length. This technique increases the sensitivity of this array platform by detecting low-expressed genes at longer exposures. It also improves the measurement accuracy of highly abundant genes by considering only values from the linear portion of dependency between the exposure times and gene intensities. As a result, the described approach improves the outcome of the subsequent steps of array data normalization and mining.

MOTIVATION: Detailed comparison and analysis of the output of DNA gene expression arrays from multiple samples require global normalization of the measured individual gene intensities from the different hybridizations. This is needed for accounting for variations in array preparation and sample hybridization conditions. RESULTS: Here, we present a simple, robust and accurate procedure for the global normalization of datasets generated with single-channel DNA arrays based on principal component analysis. The procedure makes minimal assumptions about the data and performs well in cases where other standard procedures produced biased estimates. It is also insensitive to data transformation, filtering (thresholding) and pre-screening.